Allele Registry

Canonical Allele Identifier: PA645448187

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000435140

ClinVar Variation:

376068

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.His1112Tyr	CA16602530 NM_001127500.3:c.3334C>T